ENST00000650793.2:n.577A>T
|
|
|
ENST00000697612.1:n.1255A>T
|
|
|
ENST00000374881.3:c.386A>T
|
ENSP00000364015.2:p.Lys129Met
|
|
ENST00000374882.8:c.398A>T
MANE Select
|
ENSP00000364016.4:p.Lys133Met
|
|
ENST00000650411.1:n.1719A>T
|
|
|
ENST00000650793.1:n.577A>T
|
|
|
ENST00000374881.2:c.386A>T
|
ENSP00000364015.2:p.Lys129Met
|
|
ENST00000374882.7:c.398A>T
|
ENSP00000364016.3:p.Lys133Met
|
|
ENST00000395339.7:c.326A>T
|
ENSP00000378748.3:p.Lys109Met
|
|
ENST00000484003.1:n.782A>T
|
|
|
NM_004159.4:c.386A>T
|
NP_004150.1:p.Lys129Met
|
|
NM_148919.3:c.398A>T
|
NP_683720.2:p.Lys133Met
|
|
NM_148919.4:c.398A>T
MANE Select
|
NP_683720.2:p.Lys133Met
|
|
NM_004159.5:c.386A>T
|
NP_004150.1:p.Lys129Met
|
|